EP2906115B1 - Configuration et placement spatial de capteurs d'électrode frontaux pour détecter des signaux physiologiques - Google Patents

Configuration et placement spatial de capteurs d'électrode frontaux pour détecter des signaux physiologiques Download PDF

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EP2906115B1
EP2906115B1 EP13845002.8A EP13845002A EP2906115B1 EP 2906115 B1 EP2906115 B1 EP 2906115B1 EP 13845002 A EP13845002 A EP 13845002A EP 2906115 B1 EP2906115 B1 EP 2906115B1
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electrode
exemplary
physiological
user
electrodes
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EP2906115A4 (fr
EP2906115A2 (fr
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Todd Prentice COLEMAN
Rui Ma
Michael BAJEMA
Ricardo GIL DA COSTA
Raynard FUNG
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University of California
Salk Institute for Biological Studies
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Salk Institute for Biological Studies
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/25—Bioelectric electrodes therefor
    • A61B5/279—Bioelectric electrodes therefor specially adapted for particular uses
    • A61B5/291—Bioelectric electrodes therefor specially adapted for particular uses for electroencephalography [EEG]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/316—Modalities, i.e. specific diagnostic methods
    • A61B5/369—Electroencephalography [EEG]
    • A61B5/375—Electroencephalography [EEG] using biofeedback
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    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
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    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/25—Bioelectric electrodes therefor
    • A61B5/279—Bioelectric electrodes therefor specially adapted for particular uses
    • A61B5/296—Bioelectric electrodes therefor specially adapted for particular uses for electromyography [EMG]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/316—Modalities, i.e. specific diagnostic methods
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
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    • A61B5/369—Electroencephalography [EEG]
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
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    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
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    • A61B5/369—Electroencephalography [EEG]
    • A61B5/377—Electroencephalography [EEG] using evoked responses
    • A61B5/38—Acoustic or auditory stimuli
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
    • A61B5/6802—Sensor mounted on worn items
    • A61B5/6803—Head-worn items, e.g. helmets, masks, headphones or goggles
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    • A61B5/16—Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state
    • A61B5/163—Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state by tracking eye movement, gaze, or pupil change
    • A—HUMAN NECESSITIES
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    • A61B5/16—Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state
    • A61B5/165—Evaluating the state of mind, e.g. depression, anxiety
    • A—HUMAN NECESSITIES
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    • A61B5/167—Personality evaluation
    • A—HUMAN NECESSITIES
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    • A61B5/168—Evaluating attention deficit, hyperactivity
    • A—HUMAN NECESSITIES
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    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
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    • A61B5/389—Electromyography [EMG]
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    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
    • A61B5/6813—Specially adapted to be attached to a specific body part
    • A61B5/6814—Head

Definitions

  • This patent document relates to systems, devices, and processes for acquiring and analyzing physiological signals.
  • Electroencephalography is the recording of electrical activity exhibited by the brain using electrodes positioned on a subject's scalp, forming a spectral content of neural signal oscillations that comprise an EEG data set.
  • the electrical activity of the brain that is detected by EEG techniques can include voltage fluctuations, e.g., resulting from ionic current flows within the neurons of the brain.
  • EEG refers to the recording of the brain's spontaneous electrical activity over a short period of time, e.g., less than an hour.
  • EEG can be used in clinical diagnostic applications including epilepsy, coma, encephalopathies, brain death, and other diseases and defects, as well as in studies of sleep and sleep disorders. In some instances, EEG has been used for the diagnosis of tumors, stroke and other focal brain disorders.
  • ERPs event-related potentials
  • an ERP includes an electrical brain response - a brain wave - related to the sensory, motor, and/or cognitive processing.
  • ERPs are associated with brain measures of perception (e.g., visual, auditory, etc.) and cognition (e.g., attention, language, decision making, etc.).
  • a typical ERP waveform includes a temporal evolution of positive and negative voltage deflections, termed components. For example, typical components are classified using a letter (N/P: negative/positive) and a number (indicating the latency, in milliseconds from the stimulus event), for which this component arises.
  • US 2012/253163 A1 discloses sensor designs or shapes configured to facilitate placement of sensor electrodes and, thus, proper positioning of the sensors on patients.
  • EP 1 468 646 A2 discloses a method concerning measurements by using an electrode array comprising three electrodes for central nervous system (CNS) monitoring from the forehead of a patient's head, and an electrode array for carrying out said measurements.
  • CNS central nervous system
  • US 2010/041962 A1 discloses a headset for detecting brain electrical activity.
  • Devices, systems, and techniques are disclosed for acquiring physiological signals of interest using a limited quantity of electrode sensors, e.g., which can be used to determine cognitive and/or sensory performance, psychological states, and/or behavioral preferences.
  • a physiological sensor device includes a substrate formed of an electrically insulative material and structured to allow physical contact of the device with the frontal region of the head of a user, a first electrode configured at a first location on the substrate to acquire an electrophysiological signal of the user, a second electrode configured at a second location on the substrate to acquire a second electrophysiological signal of the user as a reference signal to the electrophysiological signal, and a third electrode configured on the substrate to acquire a third electrophysiological signal of the user as an electrical ground signal, in which the third electrode is configured at a third location at least partially between the first and the second locations on the substrate, and the first location is configured posterior to the second and third locations along a sagittal direction in the frontal region when the physiological sensor device is properly placed on the frontal region of the user, and in which the device is operable when electrically coupled to an electrical circuit to detect physiological signals of the user.
  • Implementations of the physiological sensor device can optionally include one or more of the following features.
  • the first, second, and third electrodes can be linearly arranged on the substrate.
  • the detected physiological signals can be electroencephalography signals sensed from the brain of the user.
  • the detected electroencephalography signals can be associated with an event-related potential.
  • the detected physiological signals can be electromyography signals sensed from head muscles of the user associated with the user's eye blinking or facial expressions.
  • the substrate can be formed of a mechanically flexible material structured to adhere to skin or a wearable item of the user.
  • the device can further include electrical interface components formed separately on the substrate and electrically coupled to the first, second, and third electrodes, respectively, via electrically conductive conduits, in which the electrical circuit is an external electrical circuit electrically coupled to the electrical interface components via wires.
  • the electrical circuit can include a signal processing circuit formed on the exemplary mechanically flexible substrate in electrical communication with the first, second, and third electrodes via electrically conductive conduits, in which the signal processing circuit can amplify the acquired physiological signals.
  • the electrical circuit can include a transmitter unit on the substrate in electrical communication with the signal processing circuit to transmit the amplified physiological signals to at least one of a data processing unit or a remote computer system.
  • the device can further include a power supply module electrically coupled to the electrical circuit to provide electrical power to the transmitter unit.
  • the physiological sensor device can be configured as a wearable patch worn on the user's scalp. In some examples, the physiological sensor device can be configured in a region of the wearable item capable of physical contact with the user's scalp.
  • the device can further include a fourth electrode configured at a fourth location on the substrate to acquire a second electrophysiological signal of the user, and a fifth electrode configured at a fifth location on the substrate to acquire a third electrophysiological signal of the user, in which the fourth location is configured left of the first location, and the fifth location is configured right of the first location.
  • the device is implemented in a system to provide a cognitive or sensory assessment.
  • the system can include a data processing system in communication with the physiological sensor device and structured to include one or more memory units and one or more processors configured to process the detected physiological signals as physiological data to generate an information set including one or more quantitative values associated with a cognitive-sensory profile category indicative of one or more aspects of cognitive or sensory functions.
  • the one or more processors of the data processing unit can be configured to process the physiological signals detected by the physiological sensor device to generate the information set by selecting time intervals of interest within the physiological data based on the presented stimuli and the cognitive-sensory profile category, grouping, into one or more grouped data sets, the physiological data corresponding to the selected time intervals of interest, and providing a statistical measure of a relationship across or within the grouped data sets to generate the one or more quantitative values.
  • the one or more quantitative values can include a quantitative score depicting a level of one or both of cognitive and sensory performance based on at least one of the user's attention, memory, learning ability, confabulation characteristics, pattern integration ability, semantic integration ability, target detection ability, emotional valence, preference, or awareness, and wherein the quantitative score depicts the level at a particular time.
  • the system can further include a stimulus delivery device to produce a sequence of stimuli based on the cognitive-sensory profile category that is presented to the user wearing the physiological sensor device, wherein the stimuli includes at least one of a visual, auditory, olfactory, tactile, or gustatory stimulating medium, in which the physiological sensor device is interfaced to the user to detect the physiological signals exhibited by the user before, during, and after a presentation of the sequence of stimuli.
  • a stimulus delivery device to produce a sequence of stimuli based on the cognitive-sensory profile category that is presented to the user wearing the physiological sensor device, wherein the stimuli includes at least one of a visual, auditory, olfactory, tactile, or gustatory stimulating medium, in which the physiological sensor device is interfaced to the user to detect the physiological signals exhibited by the user before, during, and after a presentation of the sequence of stimuli.
  • the data processing system can include a local computer proximate to and in communication with the physiological sensor device to receive the detected physiological signals from the physiological sensor device, the local computer configured to conduct initial processing of the detected physiological signals to produce initial physiological signal data, and a remote computer in communication with the local computer via a communication network or link to receive the initial physiological signal data from the local computer and to process the initial physiological signal data to generate the information set including one or more quantitative values associated with the cognitive-sensory profile category.
  • the local computer can be a mobile communications device including a smartphone or tablet that is in wireless communications with the physiological sensor device.
  • a method to provide a cognitive or sensory assessment of a subject includes acquiring electrophysiological signals of the subject from the frontal region of the subject's head to produce physiological data using a sensor device, and processing the physiological data to generate an information set including one or more quantitative values associated with a cognitive-sensory profile category indicative of one or more aspects of cognitive or sensory functions,
  • the sensor device includes a substrate formed of an electrically insulative material and structured to allow physical contact of the sensor device with the frontal region of the head of the subject, and three electrodes including a recording electrode, a reference electrode, and a ground electrode to acquire the electrophysiological signals of the subject from three respective positions arranged on the substrate along the sagittal direction of the frontal region, in which the recording electrode is configured posterior to the ground and reference electrodes, and the ground electrode is configured between the recording and reference electrodes.
  • fMRI functional resonance magnetic imaging
  • electroencephalography electroencephalography
  • fMRI is an indirect measure of brain function by correlated metabolic function (e.g., oxygen consumption in the blood flow)
  • EEG is a direct measure of brain activity by recording changes of the electrical fields present at the scalp, deriving from electrical activity produced by neural cells.
  • Such factors can include the type of stimuli that can evoke a subject's response, duration of the stimuli, inter-stimuli interval, number of repetitions of each presentation of stimuli, the levels of the stimuli (e.g., sound, brightness or contrast levels, etc.), markers associated with the onset of presentation of each stimuli, etc., as well as the recording sensors and systems.
  • the physiological parameter(s) of use e.g., voltage, power, frequency, etc.
  • the related time window for analysis, and the analysis structure can affect the brain signal recordings and correlated cognitive evaluation. Deviations or mistakes from one or multiple of these parameters can make the difference between a useful or artifact driven, useless method.
  • Some traditional EEG recording techniques include an EEG cap covering the whole scalp, e.g., placed over the hair. These full cap EEG systems are typically neither comfortable nor aesthetically pleasing, and in some cases require the use of conductive gel, which is cumbersome to the user, and may require technical application, etc. Some EEG recording techniques do not utilize a full cap, but nonetheless include skin-mounted electrodes along with other electrodes that are spatially disparate and require a bulky headset that is not efficient in terms of portability and comfort, and/or such skin-mounted electrode systems suffer from poor signal quality revealing inadequate signal to noise ratio to optimal detection of ERPs.
  • one class of skin-mounted electronics systems used an electrode configuration having frontal electrodes and non-frontal electrodes (e.g., some placed behind the subject's ears) to acquire muscular and brain signals, but with signal resolution only able to extract coarse muscular and brain signals that included eye blink and alpha rhythm oscillations when the subject's eyes were closed, and thus incapable to adequately detect finer brain signals, such as ERPs.
  • ERPs finer brain signals
  • These techniques are either cumbersome or unable to acquire relevant brain signals to extract relevant brain signals reflective of behavioral and brain measures of interest, e.g., for characterization of cognitive and/or psychological states.
  • measurements of event-related potentials for sensory, motor and/or cognitive analysis can include techniques that capitalize in measuring transient electric shifts (e.g., ERP components) that are time-locked to the onset of a presented stimulus (e.g., visual, auditory, olfactory, gustatory, or tactile) and reflect the underlying brain activity during the investigated neuropsychological process.
  • ERP components can be indicative of multiple sensory, motor and cognitive functions.
  • the amplitude modulation and scalp distribution of a variety of ERPs represent reliable and effective brain markers for normal neuropsychological processing of a wide range of cognitive operations.
  • abnormal modulation and latencies of ERPs have been associated with various sensory and cognitive deficits linked to neuropsychiatric disorders, such as schizophrenia, Alzheimer's and Parkinson's.
  • Devices, systems, and methods are disclosed for acquiring physiological signals of interest using a limited quantity of electrode sensors, e.g., which can be used to determine cognitive and/or sensory performance, psychological states, and/or behavioral preferences.
  • a physiological sensor device includes a substrate formed of an electrically insulative material and structured to allow physical contact of the physiological sensor device with the frontal region of the head of the user, and, an optimal configuration of three electrodes on the substrate providing a minimized device footprint when the device is properly applied on the user's forehead.
  • the three electrodes include a recording electrode, a reference electrode, and a ground electrode to acquire the electrophysiological signals of the subject from three respective positions arranged on the substrate along the sagittal direction of the frontal region, in which the recording electrode is configured posterior to the ground and reference electrodes, and the ground electrode is configured between the recording and reference electrodes.
  • the disclosed technology integrates advanced cognitive neuroscience, neurophysiology, psychology and electromagnetics in optimal configurations of physiological signal detection electrodes frontally placed on the forehead to enable individual or group evaluation of a variety of cognitive aspects and physiological/health monitoring, e.g., including but not limited to, evaluation of cognitive state, knowledge, learning mechanisms, behavioral preferences, vulnerability and/or symptoms of neurological and neuropsychiatric pathologies.
  • the disclosed technology can be implemented in devices that provide easy and user-friendly operation, portability, and comfort, thereby permitting real-world usage and systematic health monitoring. Additionally, for example, the disclosed technology can be used in a variety of health, education, entertainment, and marketing applications.
  • the disclosed technology includes physiological sensor devices and methods using frontal EEG recording electrodes located on a user's forehead for versatile, rapid, and non-obtrusive physiological data acquisition (e.g., including brain signal monitoring) that do not overlap with hair.
  • the exemplary physiological sensor devices are configured to a small size and can be formed with a variety of different materials (e.g., which can be tailored for specific applications), such that the devices may be easily applied, barely or not even felt by the user, or seen by others.
  • application and operation of such devices can be performed by the user, e.g., following simple instructions, without any need for technical expertise to apply or operate the device or system. This can significantly mitigate problems present in existing systems including the need of technical expertise for operation and lack of comfort and portability of sensor devices.
  • the disclosed systems can be used by general users outside a clinical setting, with safety and accuracy, allowing for the freedom to use in a wide variety of contexts and locations, significantly reducing the cost and requirements of use for brain monitoring systems.
  • the disclosed devices and methods can be effectively used by non-experts to place the exemplary frontal electrode sensor device on the forehead of evaluated persons (or even allow the subjects to place the frontal electrodes on themselves) to optimally extract brain signals, e.g., which in some implementations can be associated with event-related potentials (ERPs), and to provide a cognitive and/or sensory profile of the subject or subjects.
  • ERPs event-related potentials
  • non-expert users need not be neuroscientists, psychologists, nor specialized physicians to implement the physiological data acquisition or interpret the generated cognitive and/or sensory profile information of the user provided by the analysis of the acquired physiological data.
  • the non-expert users can implement the disclosed systems and methods to obtain awareness and mental information profiles of the evaluated person(s), e.g., either themselves or others.
  • implementations of the disclosed devices, systems and methods can also be used within the context of brain-machine interfaces and expands the possible applications of such systems.
  • the disclosed technology includes techniques for designing an optimal sensor configuration for frontal electrode placement on a subject's forehead to accurately detect brain event-related potentials.
  • the techniques can use information from specific stimuli presentation paradigms (e.g., sensory stimulation can include visual, auditory, olfactory, gustatory or somatosensory cues) and relate the presented stimuli with recorded brain electrophysiological signals (e.g., EEG) in specific temporal windows (e.g., based on physiology data related to the neuropsychological mechanisms underlying ERPs) and spatial regions (e.g., based on neuroanatomy and on scalp topographic voltage mapping and neural generators source analysis) of interest.
  • specific stimuli presentation paradigms e.g., sensory stimulation can include visual, auditory, olfactory, gustatory or somatosensory cues
  • EEG brain electrophysiological signals
  • temporal windows e.g., based on physiology data related to the neuropsychological mechanisms underlying ERPs
  • spatial regions e.g.,
  • a physiological sensor device of the present technology includes a substrate that is formed of an electrically insulative material and structured to allow physical contact of the device with the frontal region of the head of a user, a recording electrode configured at a first location on the substrate to acquire an electrophysiological signal of the user, a reference electrode configured at a second location on the substrate to acquire a second electrophysiological signal of the user as a reference signal to the electrophysiological signal; and a ground electrode configured at a third location on the substrate to acquire a third electrophysiological signal of the user as an electrical ground signal.
  • the physiological sensor device is configured such that the first electrode is configured posterior to the third and second electrodes along a sagittal direction in the frontal region, and the third electrode is positioned at least partially between the first and the second locations on the substrate.
  • the physiological sensor device is operable when electrically coupled to an electrical circuit to detect physiological signals of the user.
  • the recording electrode, the ground electrode, and the reference electrode are linearly arranged on the substrate.
  • the arrangements of the three electrodes can be aligned in a substantially straight line along the sagittal direction of the frontal region of the user's head, with the recording electrode (e.g., at the first position) posteriorly positioned to the ground electrode, which is posteriorly positioned to the reference electrode.
  • the physiological signals detected by the exemplary frontal electrode physiological sensor device can be electroencephalography (EEG) signals sensed from the brain of the user.
  • EEG signals can be associated with an event-related potential, e.g., based on a stimulus presented to the user wearing the device on the frontal region of the user's head.
  • the physiological signals detected by the exemplary frontal electrode physiological sensor device can be electromyography (EMG) signals sensed from head muscles (e.g., including facial muscles) of the user.
  • EMG signals can be resultant from eye blinks of the user in response to an event-related potential, e.g., based on a stimulus presented to the user wearing the device on the frontal region of the user's head.
  • the exemplary frontal electrode physiological sensor device can include electrical interface components (e.g., electrical contact pads) formed separately on the substrate and electrically coupled to the recording, ground, and reference electrodes, e.g., via electrically conductive conduits, in which the electrical interface components provide an electrical coupling site to be connected (e.g., via wires) to an external electrical circuit, e.g., electrical signal amplifier and/or processing unit.
  • electrical interface components e.g., electrical contact pads
  • the exemplary frontal electrode physiological sensor device can include (i) electrical circuits for signal amplification/processing and (ii) a transmitter unit, all on the mechanically flexible substrate in electrical communication with the recording, ground, and reference electrodes, e.g., via electrically conductive conduits.
  • the sensor device is configured to record the physiological signals, amplify and process them, and transmit the recorded physiological signals to a remote device, e.g., further electrical signal processing unit, such as an amplifier, and/or a computer system.
  • the exemplary frontal electrode physiological sensor device can include a power supply module electrically coupled to the transmitter unit to provide electrical power to the transmitter unit.
  • the exemplary frontal electrode physiological sensor device can include one or more recording electrodes configured on the substrate to acquire multiple channels of electrophysiological signals of the user.
  • the exemplary frontal electrode physiological sensor device can include two additional recording electrodes (in which the device includes five electrodes: three recording electrodes, one reference electrode, and one ground electrode), in which the additional recording electrodes are proximate to the first recording electrode, ground electrode, and reference electrode arranged in the sagittal direction.
  • the two additional electrodes can be linearly arranged in the same or similar sagittal direction as the first recording electrode.
  • some of the additional electrodes can be positioned to the left of the first recording electrode, while others additional recording electrode can be positioned to the right of the first recording electrode.
  • the exemplary frontal electrode physiological sensor device is configured as an epidermal electronic sensor (EES) device in which the substrate is formed of a mechanically flexible and/or stretchable material structured to mechanically conform to and/or adhere to the skin or a wearable item of the user.
  • the device can include ultrathin silicon islands interconnected by serpentine-like wires that all rest on a biologically inert flexible polymer.
  • the epidermal physiological sensor device can include a processing unit configured on the flexible substrate and structured to include transistors, capacitors, resistors, inductors, and/and other circuit elements, etc., to process the electrophysiological signals acquired by the electrodes.
  • the processing unit of the epidermal physiological sensor device can include a processor and a memory unit.
  • the epidermal physiological sensor device can be configured to have a thickness approximate to that of a human hair.
  • FIG. 1A shows a block diagram of an exemplary embodiment of a frontal electrode sensor device 100 capable to acquire electrophysiological signals from the frontal region of the head of a subject.
  • the device 100 includes a substrate 101 of an electrically insulative material, which, in some device implementations, can be made of a mechanically flexible material.
  • the substrate 101 can include polydimethylsiloxane (PDMS), thin polyurethane with acrylic adhesive, or polyvinyl alcohol (PVA), among others.
  • PDMS polydimethylsiloxane
  • PVA polyvinyl alcohol
  • the frontal electrode sensor device 100 includes a three-electrode configuration, including a recording electrode 102, a reference electrode 103, and a ground electrode 104 configured between the recording electrode 102 and the reference electrode 103 on the basal side of the substrate 101 (e.g., the detection side of the device 100 that is in contact with the skin of the user).
  • the electrodes of the device 100 are configured along a sagittal direction in the frontal region such that the recording electrode 102 is positioned posteriorly to the ground electrode 104, which is positioned posteriorly to the reference electrode 103.
  • the ground electrode 104 is positioned at least partially between the recording electrode 102 and the reference electrode 103 on the substrate 101.
  • This recording-ground-reference electrode arrangement on the frontal region of the user's head or forehead region can minimize the overall footprint of the electrodes of the frontal electrode sensor device 100, a significant benefit for such sensor devices.
  • This recording-ground-reference electrode arrangement also provides good signal isolation between the recording electrode and the reference electrode, thus enabling more sensitive and high quality signal recording operation.
  • the general alignment of the electrodes in the sagittal direction, rather than the horizontal direction that is perpendicular to the sagittal direction, is a notable feature of this recording-ground-reference electrode arrangement and can provide beneficial sensing operations with respect to acquiring various cognitive/psychological state signals with desired accuracy.
  • the recording electrode 102, the ground electrode 104, and the reference electrode 103 are linearly arranged on the substrate 100.
  • the arrangements of the three electrodes can be aligned in a substantially straight line along the sagittal direction, with the recording electrode.
  • the three electrodes can be arranged in a nonlinear alignment that includes the recording electrode 102 positioned posteriorly to the ground electrode 104 that is positioned posteriorly to the reference electrode 103, with the ground electrode 104 at least partially between the recording electrode 102 and the reference electrode 103 on the substrate 101.
  • the frontal electrode sensor device 100 is operable to acquire electrophysiological data when electrically coupled to an electrical circuit.
  • the frontal electrode sensor device 100 includes an electrical circuit 110 on the substrate 101 electrically coupled to the recording electrode 102, the reference electrode 103, and the ground electrode 104 via individual electrical interconnects 111a, 111b, and 111c, respectively.
  • the electrical circuit 110 can include a transmitter unit in electrical communication with each of the electrodes 102, 103, and 104, e.g., via the electrically conductive conduits 111a, 111b, and 111c, respectively.
  • the device 100 can record the physiological signals and transmit the recorded physiological signals to a remote electrical signal processing unit, e.g., such as an amplifier, and/or a computer system.
  • a remote electrical signal processing unit e.g., such as an amplifier, and/or a computer system.
  • the electrical circuit 110 can include a power supply module electrically coupled to the transmitter unit to provide electrical power to the transmitter unit.
  • the frontal electrode sensor device 100 can include electrically conductive interface (contact) pads 112a, 112b, and 112c coupled to the interconnects 111a, 111b, and 111c, respectively, to provide a conductive surface to electrically interface an external electrical circuit to the electrodes 102, 103, and 104 of the device 100.
  • the external electrical circuit can be an electrical signal processing unit, e.g., such as a signal amplifier, and/or a computer system.
  • the acquired recording, reference, and ground signals are received by the signal processing unit that processes the acquired signals in a differential amplifier to amplify the difference between the recording and reference electrophysiological signals.
  • the ground signals recorded by the device 100 can be connected to the ground channel of the exemplary differential amplifier, e.g., to synchronize the signal parameters between the device 100 and the amplifier.
  • the ground electrode 104 can minimize leakage currents that may flow through the subjects via the recording system, and thus decrease any artifacts.
  • the ground electrode 104 when electrically coupled to an electrical circuit (e.g., such as the external electrical circuit), need not be connected to the ground of the electrical circuit.
  • Alternative roles of the ground electrode can include serving as an electrode for actively canceling interference.
  • the ground electrode can be electrically connected to a "driven right leg" feedback circuit, e.g., which is used in some biological signal amplification systems that measure very small electrical signals emitted by the body (e.g., EEG, EMG, ECG).
  • the frontal electrode sensor device 100 can acquire referential recordings of electrophysiological signals at the frontal region.
  • the position of the reference electrode 103, as well as its spacing with respect to the recording electrode 102 (or, in some implementations, other recording electrodes in addition to the recording electrode 102) is important, since the recordings of interest will be determined by a comparison of the activity recorded by the recording electrode 102 with respect to the activity recorded by the reference electrode 103. For example, if such signals were the same, then the detected signal reading would be zero.
  • the recording electrode 102 at a site that will allow for detection of the physiological signal of interest and position the reference electrode 103 at a substantial distance away from it at a site that will not capture the physiological signal of interest (or show a significant reduction of the signal of interest).
  • the footprint of the device 100 e.g., the occupied spatial area or "real estate" by the whole array of electrodes
  • the electrodes 102, 103, and 104 are positioned and spaced in such a manner that the signals captured are significantly different, and thereby relevant, as well as occupy a minimal total area occupied by electrodes 102, 103, and 104.
  • Methods are described in this patent document to determine optimal configurations of location and spacing are complex and can integrate psychological, neurophysiological and engineering principles.
  • the position of the reference electrode 103 is located in a substantially linear alignment with respect to the recording electrode 102, and both electrodes 102 and 103 and the ground electrode 104 are also arranged on a mid-sagittal line through the center of the frontal region, in this example.
  • the signal-processed signals are provided as physiological data, which can subsequently be processed to provide a cognitive and/or sensory profile.
  • the device 100 can be configured as an epidermal electronics physiological sensor device that can be worn directly on skin or a wearable item in contact with the frontal region.
  • the device 100 can include an additional electrically insulative layer or layers, e.g., configured on the apical side of the device 100 (e.g., the non-detection side, not in contact with the skin of the user).
  • the additional layer(s) can provide further support for the device 100.
  • the additional layer(s) can include various artistic designs, such that, when worn by the user directly on the user's skin, the device 100 can also serve as a (temporary) tattoo.
  • the device 100 can be included in a system to provide a cognitive or sensory assessment of the user.
  • Some examples of such systems are provided in PCT Patent Application PCT/US13/62491 , entitled “SYSTEMS AND METHODS FOR SENSORY AND COGNITIVE PROFILING,” filed September 27, 2013, of which the entire contents are incorporated by reference for all purposes as part of the disclosure of this patent document.
  • FIG. 1C An exemplary modular system including the frontal electrode sensor device 100 of the disclosed technology for acquisition, analysis and evaluation of physiological signals to produce an individual or group cognitive and/or sensory profile is shown in FIG. 1C .
  • the system can be implemented to provide a cognitive performance profile, a sensory performance profile, and a cognitive and sensory performance profile indicative of a subject's cognitive and/or sensory ability at the time of the assessment.
  • the type of cognitive and/or sensory profile can be selected by the user (e.g., such as the subject or a system operator) to provide a set of information including a quantitative level of cognitive and/or sensory performance, e.g., including, but not limited to attention, memory, learning, confabulation, pattern integration, semantic integration, target detection, emotional valence, preference, and state of awareness.
  • the system allows an operator to select the type of profile to be produced.
  • the system can be implemented to provide the cognitive and/or sensory profile using only physiological data acquired from the subject, e.g., with no overt behavioral response elicited from the subject.
  • the system can be implemented to provide the cognitive and/or sensory profile including previously acquired physiological data from the subject, or other subjects (e.g., group data).
  • the system can thereby, for example, be implemented to provide a cognitive and/or sensory profile about a group.
  • FIG. 1C shows a diagram of an exemplary system 10 configured to include independent modular units or devices that can be configured in a variety of different embodiments.
  • the system 10 includes a stimulus presentation module 130 to configure a specific stimulus presentation structure 131 to effectuate a presentation of a stimulus or a sequence of stimuli to a subject.
  • the stimulus presentation module 130 is embodied in a computing device, e.g., including a processor and memory unit.
  • the stimuli can include any stimulus type, including a visual, auditory, olfactory, tactile, and/or gustatory stimulating medium. Examples of visual stimuli can include images, written words, etc. Examples of auditory stimuli can include spoken words, animal vocalizations, synthesized sounds, etc.
  • the specific stimulus presentation structure 131 can be configured to include, but is not limited to, a particular type or types of stimuli, the duration of presentation of the stimuli, an inter-stimuli interval, a number of repetitions (if any) of each presentation, magnitude and/or frequency parameters associated with type of stimuli (e.g., intensity of sound or brightness or contrast level of light), a digital marker associated with the presentation of each stimuli, and a label or category of the stimuli (e.g., target or non-target).
  • type of stimuli e.g., intensity of sound or brightness or contrast level of light
  • a digital marker associated with the presentation of each stimuli
  • a label or category of the stimuli e.g., target or non-target
  • the system 10 can include a stimulus delivery module 135 in communication with the stimulus presentation module 130 to present the stimulus or the sequence of stimuli to the subject, e.g., based on the stimulus presentation structure 131.
  • the stimulus delivery module 135 can include at least one of a visual display, an auditory speaker, and an actuator to provide an olfactory, tactile, and/or gustatory stimulus.
  • the stimulus presentation module 130 and the stimulus delivery module 135 can be configured in the same device, e.g., such as a computer or mobile communication and/or computing device.
  • the system 10 includes a physiological data acquisition module 140, which can be embodied as the frontal electrode sensor device 100, to acquire physiological signals of the subject before, during, and/or after the presentation of the stimuli or sequence of stimuli via the stimulus delivery module 135.
  • the frontal electrode sensor device 100 can be implemented to acquire electrophysiological signals from the subject, e.g., including, but is not limited to, electroencephalography (EEG) signal data and electromyography (EMG) signal data.
  • EEG electroencephalography
  • EMG electromyography
  • the frontal electrode sensor device 100 can include electrophysiological sensing electrodes, e.g., EEG and/or EMG electrodes, or other types of electrophysiological sensing electrodes, coupled to a signal acquisition device, e.g., such as an analog or digital amplifier coupled to a memory.
  • electrophysiological sensing electrodes e.g., EEG and/or EMG electrodes, or other types of electrophysiological sensing electrodes
  • a signal acquisition device e.g., such as an analog or digital amplifier coupled to a memory.
  • the frontal electrode sensor device 100 can be configured in a standard EEG system with rigid electrodes attached to a cap worn by the subject.
  • the frontal electrode sensor device 100 can be configured in a portable EEG system using flexible electronics that can be worn on the subject, e.g., directly applied the subject's skin or worn in a wearable item (e.g., such as a hat) by the subject with the frontal electrode sensor device 100 in physical contact with the frontal region of the subject's scalp.
  • the frontal electrode sensor device 100 can be configured in a standard EMG system with rigid electrode or a portable EMG system using flexible electronics that can be worn on the subject, in which the frontal electrode sensor device 100 is in physical contact with the frontal region of the subject's scalp.
  • the frontal electrode sensor device 100 in the rigid electrode standard EMG system or portable flexible electronics EMG system is capable of detecting movements that can be associated with drowsiness or facial expressions of the subject.
  • the system 10 includes an analysis pre-processing module 145 to receive the acquired physiological signals as data, and in some implementations, to perform pre-processing analysis techniques on the acquired data.
  • the analysis pre-processing module 145 can be implemented to identify exemplary onset markers in the acquired electrophysiological data (e.g., EEG data), segment the electrophysiological data, filter raw signal data to increase signal to noise, etc.
  • the analysis pre-processing 145 can be embodied in a computer device in communication with the exemplary device 100.
  • the analysis pre-processing module 145 can be configured in the same exemplary device that embodies the physiological acquisition module 140 (e.g., such as the frontal electrode sensor device 100).
  • the system 10 includes a profile generation module 150 to process the physiological data acquired by the frontal electrode sensor device 100 to provide a cognitive or sensory assessment of the subject, or in some examples, of a group.
  • the profile generation module 150 processes the physiological to generate an information set 152 that includes one or more quantitative values that are associated with the selected profile category, e.g., such as a knowledge evaluation or state of awareness profile.
  • the information set 152 provides more than a measure of psychological and neurophysiological natural events.
  • the profile can provide an individual (or group) assessment of one's (or group's) level of knowledge of specific issues (e.g., determination of a given person knowledge about a specific topic, event, learned skill or even preference) and/or state of conscious (or unconscious) awareness.
  • the profile generation module 150 can also include processing behavioral signal data, e.g., acquired from the subject or group of individuals that include or do not include the subject, from a behavioral signal data acquisition module (not shown in FIG. 1C ) to provide the cognitive or sensory assessment of the subject or of a group.
  • processing behavioral signal data e.g., acquired from the subject or group of individuals that include or do not include the subject, from a behavioral signal data acquisition module (not shown in FIG. 1C ) to provide the cognitive or sensory assessment of the subject or of a group.
  • FIG. 1D shows a process diagram of an exemplary method 170 to generate the information set associated with the cognitive and/or sensory profile, e.g., implemented by the profile generation module 150, using the physiological data acquired by the exemplary frontal electrode sensor device 100.
  • the method 170 can also include using behavioral signal data acquired from the subject, or group of individuals that include or do not include the subject.
  • the behavioral signal data can be processed in implementations of at least some or all of the processes of the method 170.
  • the method 170 can include a process 171 to identify a time interval associated with the physiological signals (and/or behavioral signal data) based upon the presented stimuli and the selected profile category.
  • a time interval can include contiguous, discontinuous, continuous, discrete, or single time points.
  • the method 170 can include a process 172 to group the data (e.g., physiological and/or behavioral) corresponding to the time interval into one or more grouped data sets.
  • the process 172 can include grouping the physiological data (and/or behavioral data) based on a pre-assigned category of the individual stimulus and/or an associative relationship of consecutive stimuli.
  • the method 170 can include a process 173 to provide a statistical measure of a relationship across or within the grouped data sets to generate the one or more quantitative values for the selected profile category.
  • the method 170 can include a process to enhance the signal of the physiological (and/or behavioral data) in the grouped data sets.
  • FIG. IE shows a process diagram of an exemplary method 180 to generate the information set associated with the cognitive and/or sensory profile using previous individual and/or group information, e.g., implemented by the profile generation module 150, using the physiological data acquired by the exemplary frontal electrode sensor device 100.
  • the method 180 can also include using behavioral signal data acquired from the subject, or group of individuals that include or do not include the subject.
  • the method 180 can include a process 181 to identify a time interval associated with the physiological signals (and/or behavioral signal data) based upon the presented stimuli and the selected profile category.
  • the method 180 can include a process 182 to group the data, e.g., physiological data (and/or behavioral data), corresponding to the time interval into one or more grouped data sets.
  • the process 182 can include grouping the physiological data (and/or behavioral data) based on a pre-assigned category of the individual stimulus and/or an associative relationship of consecutive stimuli.
  • the method 180 can include a process 182 to provide a statistical measure of a relationship across or within the grouped data sets using previous physiological data (and/or behavioral data) acquired from the subject and/or other subjects (e.g., including one or more groups) to generate the one or more quantitative values for the selected profile category.
  • FIG. IF shows a process diagram of an exemplary method 190 to generate the information set associated with the cognitive and/or sensory profile using a guided classification technique, e.g., implemented by the profile generation module 150, using the physiological data acquired by the exemplary frontal electrode sensor device 100.
  • the method 190 can also include using behavioral signal data acquired from the subject, or group of individuals that include or do not include the subject.
  • the method 190 can include a process 191 to identify a time interval associated with the physiological signals (and/or behavioral signal data) based upon the presented stimuli and the selected profile category.
  • the method 190 can include a process 192 to group the data, e.g., physiological data (and/or behavioral data) corresponding to the time interval into one or more initial grouped data sets.
  • the method 190 can include a process 193 to classify each stimulus of the sequence of stimuli presented to the subject using a statistical test involving the initial grouped data sets.
  • the method 190 can include a process 194 to re-group the physiological data (and/or behavioral data) corresponding to the time interval into one or more grouped data sets based on the classified stimuli.
  • the method 190 can include a process 195 to provide a statistical measure of a relationship across or within the grouped data sets to generate the one or more quantitative values for the selected profile category.
  • the profile generation module 150 can implement guided classification algorithms with context specific parameters to guide and choose from a variety of classification and statistical methods, e.g., including, but not limited to, ANOVA based techniques 151a, support vector machine based techniques 151b, and minimum description length techniques 151c, among others.
  • the profile generation module 150 can be embodied on a computer system or communication network (referred to as 'the cloud') that includes one or more remote computational processing devices (e.g., servers in the cloud).
  • the system 10 can be configured to include a brain-machine interface module 155 to refine the generated cognitive and/or sensory profiles and/or actuate an interaction between a user and a machine.
  • the brain-machine interface module 155 can provide a feedback delivery of a new stimulus or multiple stimuli to the stimulus presentation module 130 based on the cognitive and/or sensory profile of an individual subject or group subject that has been generated from the profile generation module 150, e.g., from an on-going implementation of the system 10 or a previously generated profile by the system 10.
  • the brain-machine interface module 155 can adaptively change or design stimuli paradigms that optimally extract information from the subject that is analytically processed to maximize a desired objective.
  • some implementations of the brain-machine interface module 155 can include, but are not limited to, assisted-learning and target detection applications.
  • the profile generation module 150, the stimulus presentation module 130, the stimulus delivery module 135, and the brain-machine interface module 155 can be embodied in a single computing system, e.g., a desktop computer, a laptop computer, or a mobile communications device including a smartphone or tablet, that interacts with the physiological data acquisition module 140 (e.g., the frontal electrode sensor device 100).
  • the modules 150, 130, 135, and 155 can be configured in two or more computing devices in communication with each other and including various combinations of the modules 150, 130, 135, and 155.
  • the system 10 can be configured to just include the physiological data acquisition module 140 and the profile generation module 150.
  • the system 10 can use environmental stimuli (e.g., light, sounds, smells, tastes, and/or tactile contacts) that are presently available in the subject's surroundings.
  • a method to provide a cognitive or sensory assessment of a subject using the physiological sensor devices of the disclosed technology includes acquiring electrophysiological signals of the subject from the frontal region of the subject's head to produce physiological data using a sensor device, and processing the physiological data to generate an information set including one or more quantitative values associated with a cognitive-sensory profile category indicative of one or more aspects of cognitive or sensory functions.
  • the sensor device includes a substrate formed of an electrically insulative material and structured to allow physical contact of the sensor device with the frontal region of the head of the subject, and three electrodes including a recording electrode, a reference electrode, and a ground electrode to acquire the electrophysiological signals of the subject from three respective positions arranged on the substrate along the sagittal direction of the frontal region, in which the recording electrode is configured posterior to the ground and reference electrodes, and the ground electrode is configured between the recording and reference electrodes.
  • the method can further include presenting a sequence of stimuli to the subject, the sequence of stimuli based on the cognitive-sensory profile category, in which the acquiring the physiological signals is implemented before, during, and after the presenting the sequence of stimuli.
  • the method can further include selecting the cognitive-sensory profile category from among a cognitive performance profile, a sensory performance profile, and a cognitive and sensory performance profile.
  • the sequence of stimuli can include at least one of a visual, auditory, olfactory, tactile, or gustatory stimulating medium based on the selected cognitive-sensory profile category.
  • the one or more quantitative values can include a quantitative score depicting a level of one or both of cognitive and sensory performance based on at least one of the subject's attention, memory, learning ability, confabulation characteristics, pattern integration ability, semantic integration ability, target detection ability, emotional valence, preference, or awareness state, and wherein the quantitative score depicts the level at a particular time.
  • the method can further include identifying a time interval associated with the physiological signals based on the cognitive-sensory profile category, grouping the physiological data corresponding to the time interval into one or more grouped data sets, and providing a statistical measure of a relationship across or within the grouped data sets to generate the one or more quantitative values for the selected cognitive-sensory profile category.
  • FIG. 1G shows an illustrative diagram depicting an exemplary method 160 to determine optimal spatial placement of frontal electrode sensors to acquire EEG event-related potentials.
  • the method 160 includes presenting the stimulus presentation structure 131 using the stimulus delivery module 135 to a subject, who can wear a conventional 'full scalp' EEG acquisition device with electrodes located at positions across the subject's head.
  • the stimulus presentation structure 131 can be used to effectuate a presentation of a stimulus or a sequence of stimuli to a subject.
  • the EEG response of the subject to the presentation of the stimulus or sequence of stimuli is acquired using the 'full scalp' EEG acquisition device to acquire the EEG signal data from a plurality of electrodes across a plurality of regions of the brain, e.g., including frontal, parietal, occipital, and temporal cerebral regions.
  • the acquired data can be analyzed using the pre-processing module 145 to implement pre-processing analysis techniques on the acquired data.
  • the pre-processing analysis techniques include producing one or more topographical voltage maps 146 of the electrophysiological data, e.g., which can be over different temporal and/or spatial parameters.
  • the pre-processing module 145 can utilize the data produced in the topographical voltage map(s) 146 in data processing techniques to optimize spatial arrangement parameters of the electrodes that can be included in a frontal electrode physiological sensor device.
  • the spatial arrangement parameters can include the number of electrodes, electrode type and size, location / placement of each electrode, spacing between the electrodes, etc.
  • determination of the location and/or placement of the electrodes can be based on the type of signal to be recorded (e.g., signal of interest, a reference signal, and ground signal).
  • the electrode location and/or placement parameters can include relative distances of the electrodes, particular placements of the electrodes with respect to the subject's frontal region of his/her head, etc.
  • such parameters e.g., type, quantity, size, placement, relative position, etc.
  • parameters account for topography, amplitude, and localization of physiological signals of interest (e.g., including event-related potential brain markers), as well as specific metal conductance, resistance, and spacing parameters.
  • the described exemplary implementations include eliciting and extracting various brain ERPs (e.g., P300, notion/feeling of 'reward', and mismatch negativity) measured by EEG recordings using visual stimuli and auditory stimuli to produce an information set providing quantitative values corresponding to the cognitive performance, sensory performance, and/or awareness state profile.
  • eye tracking data can be used in addition to the exemplary EEG recording physiological data acquired by the exemplary frontal electrode physiological sensor devices for providing the cognitive and/or sensory assessment.
  • exemplary ERPs used in the exemplary implementations include, but are not limited to, the P300, notion/feeling of 'reward', and the mismatch negativity.
  • Other exemplary ERPs that can be implemented to provide an exemplary cognitive-sensory profile using the disclosed technology can include the N400, among others.
  • exemplary applications of the exemplary frontal electrode physiological sensor devices with the disclosed methods and systems use the exemplary P300, 'reward', and mismatch negativity ERPs as illustrative examples to described how the exemplary methods can be implemented, e.g., stimuli design and presentation, physiological signal (e.g., EEG) recording, physiological data (e.g.,. ERP) analysis, and cognitive and/or sensory profile generation (e.g., including inferred cognitive and/or awareness states).
  • physiological signal e.g., EEG
  • physiological data e.g.,. ERP
  • cognitive and/or sensory profile generation e.g., including inferred cognitive and/or awareness states.
  • the disclosed cognitive and/or sensory profile generation methods and systems can be used to measure brain markers, but in addition, it evaluates and transforms this information into a new type of purposeful data that creates an individual knowledge evaluation and/or state of awareness profile. Moreover, in some implementations, for example, the disclosed methods and systems can use this profile to guide a brain-machine interface system.
  • the P300 is a brain endogenous response characterized by a positive-going electrical response between 300 and 800 ms, with a central-parietal maxima scalp distribution.
  • the P300 is inversely correlated with an item's subjective probability of occurrence. For example, the P300 has been used in visual target detection tasks, where the target elicits higher amplitude P300s than the other items.
  • an arbitrary visual cue e.g., green circle
  • the tested subjects were instructed to associate it with a notion or feeling of "reward”.
  • the subjects were instructed to associate the exemplary green circle with a cue of good task performance and informed that the occurrence of the cue during testing would be correlated with increase compensation after the test, thus, creating an association of this arbitrary cue with a notion of "reward”.
  • the brain responses to this "reward” stimulus was subsequently analyzed.
  • the exemplary illustrations of the disclosed methods using P300 illustrates the broad applicability of the methods across various EEG recording techniques.
  • the method can be applied to assess cognitive and/or sensory profiles using brain data (e.g., EEG signals) recorded using a traditional rigid electrodes EEG system with the disclosed frontal electrode configurations, as well as with EEG data acquired using wearable, flexible epidermal electronic sensors with the disclosed frontal electrode configurations.
  • brain data e.g., EEG signals
  • EEG data acquired using wearable, flexible epidermal electronic sensors with the disclosed frontal electrode configurations.
  • the stimuli were comprised of multiple image categories, e.g., including animals; cars; faces; flowers; houses; random objects; motorcycles; airplanes; and buildings.
  • the exemplary pool of stimuli was obtained from various resources.
  • FIG. 2 shows a diagram of an exemplary sequence of presented visual stimuli.
  • This diagram portrays images of specific presented exemplars and the pre-programmed pseudo-randomized order of presentation Having the adequate stimuli presentation structure for each solution is an intrinsic and important part of the exemplary method.
  • the relevant aspect is the distinction between the images that represent pre-determined "Targets" versus all other images (labeled as “Distractors”) and versus the green circle previously associated with an indication of "Reward”.
  • the adequate stimuli structure e.g., in this case, the specific content of images of interest as targets embedded in a sequence of other images, location of presentation, timing of presentation, timing of inter-stimulus interval, etc.
  • the described specialized subsequent analysis are important in the exemplary method to how to use relevant brain markers, e.g., in this exemplary case, the P300 and the "reward" elicited ERPs, to evaluate and determine individual knowledge, levels of attention and preferences to specific items.
  • the desired relative luminance was set to be a value equal to 120.
  • the script measured the initial relative luminance of each image, it either added or subtracted RGB values to every pixel within the image in order to achieve an average relative luminance of 120. Images were then saved at 100% quality.
  • This exemplary process After controlling for luminance, another computer implemented process (e.g., programmed using a MATLAB script) was used to place a centrally positioned fixation dot on each stimulus exemplar. For example, this helped the subject to maintain fixation and minimize any frequent eye saccades.
  • This exemplary process first measured the dimensions of an uploaded image. It used these measurements to calculate the center of the image and subsequently create a fixation dot using the standard equation of a circle. Pixels within a seven pixels length radius around the center were altered by changing the pixels' red gun to 255, the green gun to 0, and the blue gun to 0.
  • the visual stimuli for the fixation dot and an arbitrary visual cue for "reward" were created.
  • a computer implemented process e.g., programmed using a MATLAB script
  • a grey background image e.g., red gun equal to 150; green gun equal to 150; blue gun equal to 150
  • the exemplary script ran a nested for-loop using the standard equation of a circle to alter pixels within a seven pixels length radius to red, e.g., by changing the image's red gun to 255, the green gun to 0, and the blue gun to 0.
  • imaging software was used to create a green circle (e.g., red gun equal to 0; green gun equal to 255; blue gun equal to 0) on a 350 ⁇ 350 pixels grey background (e.g., red gun equal to 150; green gun equal to 150; blue gun equal to 150) background.
  • the exemplary stimulus presentation paradigm that was used in this example stimuli presentation process was programmed using Cogent 2000, and included presenting visual stimuli serially with brief presentation durations.
  • the pool of stimuli, not including the fixation dot and green circle was divided into two groups, one for each of the two recording techniques.
  • Each technique included 900 stimuli, for a total of 1800 stimuli across recording techniques.
  • the 900 stimuli, including targets and distractors, each presented for 100 ms were divided into three presentation blocks.
  • the green circle stimulus presentation lasted 1000 ms and was shown 30 times within each presentation block.
  • the fixation dot was visible during every target trial, distractor trial, and inter-stimulus interval (ISI).
  • ISI inter-stimulus interval
  • targets were human faces.
  • targets were cars.
  • targets were animals.
  • the order of the presentation blocks within each technique was also randomized. Presentation blocks were never repeated consecutively (e.g., block 1, block 2, block 3, block 3, block 2, block 1, block 1, block 3, block 2) across techniques. Because the subject was instructed to count how many times he/she saw a particular target, the correct number of targets was varied for each block. For example, in block 1 (target: faces), there were 56 targets and 244 distractors. For example, in block 2 (target: cars), there were 62 targets and 238 distractors. For example, in block 3 (target: animals), there were 60 targets and 240 distractors.
  • Distractors were composed of all of the non-target object categories. For example, in block 1 (target: faces), the distractors included cars, animals, flowers, houses, etc.
  • the exemplary MATLAB code began by prompting the experimenter to enter the subject's initials and choose which block to present. Depending on the chosen block number, the script calculated which object category would be target, the number of targets, and the number of distractors. Afterward, it randomized the order of stimulus presentation using the MATLAB randperm() function. It ran the randperm() function twenty times to better randomize the presentation sequence. Then, it created inter-stimulus intervals (ISI) for each trial using the randi() function. The inter-stimulus intervals ranged from 500 ms to 600 ms.
  • ISI inter-stimulus intervals
  • a log file was configured and initialized within Cogent 2000. This log file was used to create a history of every trial regarding its stimulus type (e.g., target, distractor and green circle). Subsequently, the stimuli were loaded into memory buffers. The aforementioned steps were executed prior to stimulus presentation, e.g., to reduce computational load and increase latency precision.
  • the stimulus presentation included a for-loop that iterated down the pre-determined presentation order. For example, based on the value of the current stimulus in the presentation order, the computer implemented process calculated its stimulus type and sent the appropriate information regarding its stimulus type to the log file and parallel port, whose trigger was sent to the EEG recording computer. Then, the program presented the ISI. At the end of each presentation, the parallel port was reset to zero to prepare for the next trial.
  • each subject was seated in a chair in a recording chamber to begin an EEG capping process.
  • this process involved placing a traditional EEG cap on the subject's head and securing it with an elastic chin strap. In some examples, either a 56 cm or a 58 cm diameter cap was used, e.g., based on the estimated size of the subject's head.
  • Signa electrode gel e.g., from Parker Laboratories
  • Signa electrode gel was injected using a curved, plastic syringe under each of the cap's electrodes to create a conductive bridge between the electrode itself and the subject's scalp.
  • the subjects were seated in front of the presentation monitor and asked to just maintain visual fixation on a red, central fixation dot throughout the duration of the experiment and restrict their motor movements as much as possible to prevent motion artifacts in the neurophysiological data. Afterwards, the recording room's lights were then dimmed, and the stimulation process and EEG recordings began.
  • a traditional EEG system with rigid electrodes was used to acquire brain waves.
  • the exemplary EEG system included a BrainAmp DC 32-channel system; BrainVision Recorder; Fast n Easy 32-channel EEG recording cap size 56 cm; Fast n Easy 32-channel EEG recording cap size 58 cm; PCB Ribbon Cable for BrainCap-MR with 5k resistors; and BrainCap MR Box 1.2.
  • Data analysis techniques included multiple steps and processes, e.g., including the processing of marker data and individual statistical analysis.
  • the exemplary EEG recordings system produced three files: data file (.eeg), header file (.vhdr), and marker file (.vmrk).
  • the marker files contained the event triggers for each stimulus onset.
  • the Cogent 2000 log file was used to hold more readable information regarding an exemplar's stimulus type (e.g., target, distractor, or green circle).
  • a process e.g., programmed using a MATLAB script
  • the first marker in the .vmrk file was replaced by the first marker in the log file; the second marker in the .vmrk file was replaced by the second marker in the log file, etc.
  • ERP Integrated Multimedial-Reliable Statistical Analysis
  • exemplary analytical methods to calculate ERPs (e.g., using BrainVision Analyzer 2). For example, ERP waveforms were calculated for "Targets", “Distractors” and "Reward”. Subsequently, for example, from each ERP waveform the spatial location and timing of the ERP components of interest were determined. For example, for each time-window of interest, topographic voltage maps for each ERP component of interest were calculated using the available voltage information from every electrode in the EEG cap (total 32 electrodes). In the exemplary implementations described herein, a combination of MATLAB and Statsoft Statistica (version 8.0) software was used for statistical analyses.
  • the determination of an optimal electrode placement using our method can be obtained by integrating all this information, for example: (i.) Sensory or cognitive neuropsychological mechanism of interest; (ii.) Designing an adequate stimulus presentation and delivery method for eliciting the neuropsychological mechanism of interest; (iii.) Tag chronological markers associated with onset of stimulus presentation; (iv.) Record EEG signals from the subject during stimulation; (v.) Analyze EEG data and calculate ERPs for each condition / marker of interest; (vi.) Identify ERP components of interest in every channel of the dataset; (vii.) For each component of interest, determine latency (time of occurrence) and spatial distribution (which electrodes show the ERP of interest); (viii.) Based on the latency of each component of interest, determine a time-window of occurrence for each component and create topographic voltage maps; (ix.) For each ERP component of interest, investigate where in the scalp it has a significant "expression" (i.e., in which electrodes is it present and how is its voltage distributed in the topographic voltage map
  • the reference electrode is positioned away from the recording electrode and in a location where the "brain function of interest" is minimal or provides no expression. In this way, when one is differentiating the reference signal from the recording signal, it wouldn't be 'subtracting' anything of interest.
  • large separations use relatively large amounts of spatial area on the forehead.
  • a minimal configuration of electrodes are placed on the frontal region of the subject that require the minimal amount of spatial area (e.g., placing the recording and reference electrodes close together) while still providing reliable physiological signal readings and detection.
  • the disclosed electrode configuration optimization method was implemented to obtain such configurations.
  • the accuracy of an optimal classifier is a monotonic function of the energy in the difference between the scalp potential of the recording electrode under the null hypothesis (for example the "Distractors” in the P300 paradigm) and scalp potential of the recording electrode under the alternate hypothesis (for example the "Targets” in the P300 paradigm).
  • a criterion for maximizing classification accuracy which is equivalent to maximizing the energy in the difference between the recording electrode's potential in "Targets" and "Distractors” setting.
  • an electrode pair is placed across isopotential lines (e.g., same or identical voltage potential values), then the potential difference is sensitive to current flow from regions of high to low, or low to high, potentials. This is referred to as placing the electrode pair along a gradient potential. However, if the bipolar pair is placed along an isopotential line, then a zero, or close to zero differential potential is recorded. Maximizing energy in the difference is done when the placement of the frontal electrodes is along the gradient of the frontal scalp distribution of the brain signal of interest.
  • isopotential lines e.g., same or identical voltage potential values
  • the gradients of the voltage scalp distribution are oriented vertically.
  • the recording electrode, ground electrode and reference electrode should be placed from top to bottom (e.g., from the top of the forehead towards the nose), which is across the isopotential line.
  • placing the recording electrode, ground electrode, and reference electrode orthogonal to that direction will result in a degraded classification performance - approaching that of chance.
  • the disclosed top-to-bottom (e.g., top of the forehead towards the nose) frontal region electrode configuration also is capable of detecting relevant neurophysiological signals of the underlying functional-neuroanatomy (e.g., the human brain has symmetrical hemispheres along a mid-sagittal line and that many sensory and cognitive processes occur with functional and anatomical hemispheric asymmetries).
  • relevant neurophysiological signals of the underlying functional-neuroanatomy e.g., the human brain has symmetrical hemispheres along a mid-sagittal line and that many sensory and cognitive processes occur with functional and anatomical hemispheric asymmetries.
  • placing the electrodes along the brain axial (or transversal) plane e.g., along the forehead from left to right
  • the exemplary methodology of the disclosed technology also suggests that the greater the expression of an event-related potential is in frontal voltage scalp distributions, the easier it is to classify.
  • FIG. 3A shows diagrams illustrating an exemplary frontal electrode configuration using a conventional EEG system and exemplary results from its implementation for detecting the EEG signal response to P300 ERP detection of "Targets" and "Distractors".
  • an image 300 is shown of an exemplary subject wearing a conventional EEG rigid electrode detection cap 301.
  • a diagram 305 is shown depicting a tridimensional reconstruction and top and right side schematical views of the 32 electrodes' location in the conventional EEG rigid electrode detection cap 301.
  • a diagram 306 is shown depicting a two dimensional views of the 32 electrodes' location in the conventional EEG rigid electrode detection cap 301. As shown in FIG.
  • a diagram 310 shows an exemplary topographic voltage map (e.g., with indication of the frontal expression of ERP of interest, in this exemplary case, a P300 ERP for "Targets" in an exemplary analyzed time-window (e.g., 344-396 ms).
  • a data plot 315 shows the exemplary ERP waveforms from a frontal electrode (Fp1) for both "Targets"(- red line) and "Distractors” (- black line).
  • Fp1 frontal electrode
  • - red line a frontal electrode
  • - black line a hemispherically symmetric distribution is present, where isopotential lines are on the transversal plane.
  • the frontal electrodes are placed orthogonal to the transversal plane, across the isopotential line.
  • FIG. 3B shows diagrams illustrating an exemplary frontal electrode configuration using an exemplary three-electrode frontal sensor device and exemplary results from its implementation for detecting the EEG signal response to P300 ERP detection of "Targets" and "Distractors".
  • FIG. 3B shows a diagram 320 of the frontal electrode sensor device 100 in physical contact with the frontal region of a subject's head and aligned across an isopotential line (e.g., with the recording electrode placed toward the top of the forehead, the reference electrode placed toward the nose on the forehead, and the ground electrode placed between the recording and reference electrodes).
  • FIG. 3B shows diagrams illustrating an exemplary frontal electrode configuration using an exemplary three-electrode frontal sensor device and exemplary results from its implementation for detecting the EEG signal response to P300 ERP detection of "Targets" and "Distractors”.
  • FIG. 3B shows a diagram 320 of the frontal electrode sensor device 100 in physical contact with the frontal region of a subject's head and aligne
  • FIG. 3B shows a data plot 325 of the ERP waveforms acquired from the frontal recording electrode (e.g., Rec F1 - white circle 102) for both "Targets”- red line and “Distractors” - black line.
  • the disclosed frontal electrode configuration in the 3-electrode sensor devices can detect the ERPs of interest (“Targets” and “Distractors”) as reliably as a full cap traditional EEG system.
  • the polarity of the ERPs (“Targets” and “Distractors”) is reversed between the exemplary frontal system and the EEG cap frontal electrode due to the relative position of the "Reference" electrode in regards to the "Recording" electrode.
  • the "Recording" electrode occupies a significantly more anterior position than the "Reference”, while in the exemplary system shown in FIG. 3B , the "Reference” electrode is in a lower and slightly more anterior position than the "Recording" electrode.
  • the disclosed frontal electrode configurations were implemented across different electrode types and materials, e.g., including EEG recording technologies using a traditional full EEG cap with rigid electrodes and three classes of frontal electrode sensor technologies containing a ground, reference, and recording electrode, using: (1) exemplary rigid sensors (e.g., obtained from Brain Products); (2) exemplary custom-designed rigid sensors; and (3) an exemplary epidermal electronics sensor device with flexible electronics electrodes.
  • exemplary rigid sensors e.g., obtained from Brain Products
  • custom-designed rigid sensors e.g., obtained from Brain Products
  • an exemplary epidermal electronics sensor device with flexible electronics electrodes e.g., epidermal electronics sensor device with flexible electronics electrodes.
  • BrainVision Analyzer exported text files containing data values in regards to condition, subject, trial, electrode channel, and mean voltage amplitude.
  • the mean voltage amplitude was extracted from a frontal electrode for the following time intervals of interest, for example: Targets and Distractors, 400 ms to 500 ms after stimulus onset; Reward stimuli, 456 ms to 556 ms after stimulus onset.
  • the same exemplary parameters were used in all the exemplary techniques (e.g., the exemplary rigid electrodes from Brain Products, the exemplary custom-designed rigid electrodes, and the exemplary EES flexible electrode sensors).
  • these data were written to text files by BrainVision Analyzer and subsequently loaded into an exemplary MATLAB program that we created to sort and organize the data in a more accessible format.
  • the exemplary script allowed an easier data selection process by column, e.g., using MATLAB's variable editor. After selecting, data were put into Statistica data spreadsheets.
  • one-way (factor 1: condition) repeated measures ANOVAs were performed on each Statistica spreadsheet for the comparison between distractors and targets for each of the EEG recording techniques.
  • each spreadsheet was specific to the following: 1) EEG technology; and 2) comparison: distractors vs. targets.
  • a T-test was performed comparing the reward's extracted mean amplitude values against zero.
  • each spreadsheet was specific to the following: 1) EEG technology; and 2) comparison: reward vs. zero.
  • FIGS. 4A and 4B show exemplary three-electrode configurations using rigid electrodes along a gradient potential configuration and along an isopotential configuration, respectively.
  • a gradient potential configuration (referred to here as "vertical-sagittal") used three electrodes placed from the top of the forehead towards the nose, as follows: "Recording F1" electrode, "Ground” electrode, 'Reference” electrode, as shown in FIG.
  • an isopotential configuration (referred here as "horizontal-transverse") used three electrodes placed along the forehead from left to right, as follows: “Reference” electrode, "Ground” electrode, "Recording F1" electrode, as shown in FIG. 4B .
  • FIG. 5 shows data plots of an exemplary EEG online recording acquired using the exemplary rigid electrodes (e.g., obtained from Brain Products) before stimuli presentation for both gradient potential and isopotential configurations.
  • the data plot 510 shows the exemplary EEG data for the isopotential configuration of the exemplary three-electrode frontal rigid EEG sensor.
  • the data plot 520 shows the exemplary EEG data for the gradient potential configuration of the exemplary three-electrode frontal rigid EEG sensor. Eye blinks were used to better illustrate the signal-to-noise (SNR) ratio of the response in this example.
  • SNR signal-to-noise
  • FIG. 6 shows data plots of an exemplary EEG online recording acquired using the exemplary rigid electrodes during an exemplary stimuli presentation for both gradient potential and isopotential configurations.
  • the data plot 610 shows the exemplary EEG response data for the isopotential configuration of the exemplary three-electrode frontal rigid EEG sensor.
  • the data plot 620 shows the exemplary EEG response data for the gradient potential configuration of the exemplary three-electrode frontal rigid EEG sensor. Eye blinks were used to better illustrate the signal-to-noise (SNR) ratio of the response in this example.
  • SNR signal-to-noise
  • FIG. 7A shows an exemplary data plot of ERP waveforms acquired using the exemplary rigid electrodes from a single subject for "Targets" (red line) and “Distractors” (black line) using both the “vertical-sagittal” configuration (gradient potential configuration, shown by thicker lines) and the “horizontal-transverse” configuration (isopotential configuration, shown by thinner lines).
  • FIG. 7B shows an exemplary data plot of ERP waveforms acquired using the exemplary rigid electrodes from a single subject for "Reward” (blue line) using both the “vertical-sagittal” configuration (gradient potential configuration, shown by thicker lines) and the “horizontal-transverse” configuration (isopotential configuration, shown by thinner lines).
  • the disclosed three-electrode frontal configuration using the gradient potential configuration is capable of efficient ERP detection using rigid electrodes.
  • rigid forehead sensors were fabricated using an exemplary micro-fabrication method involving gold, polyimide, and Tegaderm.
  • the exemplary micro-fabrication method included a first process to deposit Au (e.g., 200 nm) onto adhesive polyimide tape by E-beam evaporation or sputtering.
  • the exemplary micro-fabrication method included a second process to cut polyimide tape into small rectangle, e.g., with aspect ratio of 1:3.
  • the 3 square portions are called left, middle, and right, with adhesive side facing up.
  • the exemplary micro-fabrication method included a third process to fold the left of the tape towards the middle and adhere firmly.
  • the exemplary micro-fabrication method included a fourth process to attach pre-cut anisotropic conductive film (ACF) lead onto the mid-line of the right square, with the conductive side of the ACF facing up.
  • the exemplary micro-fabrication method included a fifth process to fold the right square towards the middle square and adhere firmly. So far, for example, one single-lead electrode is made.
  • the exemplary micro-fabrication method included a process to repeat the first to fifth processes, e.g., until 3 single-lead electrodes are made.
  • the exemplary micro-fabrication method included a process to peel a piece of Tegaderm open to halfway.
  • the exemplary micro-fabrication method included a process to attach the 3 single-lead electrodes on the adhesive side of the Tegaderm, along the mid-line.
  • the exemplary micro-fabrication method included a process to re-attach (e.g., slowly) the Tegaderm back to its waxy paper.
  • the exemplary micro-fabrication method included a process to solder the 3 ACF leads onto 3 "Deutsches Institut für Normung" (DIN) lead-wire cables.
  • FIG. 8 shows an image 801 of the exemplary fabricated, custom-designed rigid electrodes.
  • the application of this exemplary frontal three-electrode gradient potential (vertical-sagittal) configuration is illustrated on an exemplary subject.
  • FIG. 9A shows an exemplary data plot of ERP waveforms acquired using the exemplary rigid electrodes (e.g. obtained from Brain Products) from a single subject for "Targets" (red line) and “Distractors” (black line) using the “vertical-sagittal” configuration (gradient potential configuration).
  • FIG. 9B shows an exemplary data plot of ERP waveforms acquired using the exemplary rigid electrodes (e.g. obtained from Brain Products) from a single subject for "Reward” (blue line) using both the “vertical-sagittal” configuration (gradient potential configuration).
  • FIG. 9A shows an exemplary data plot of ERP waveforms acquired using the exemplary rigid electrodes (e.g. obtained from Brain Products) from a single subject for "Targets" (red line) and “Distractors” (black line) using the “vertical-sagittal” configuration (gradient potential configuration).
  • FIG. 9B shows an exemplary data plot of ERP waveforms acquired using the exemplary rigid electrodes (e.g. obtained from
  • FIG. 9C shows an exemplary data plot of ERP waveforms acquired using the exemplary custom-designed rigid electrodes from a single subject for "Targets" (red line) and “Distractors” (black line) using the “vertical-sagittal” configuration (gradient potential configuration).
  • FIG. 9D shows an exemplary data plot of ERP waveforms acquired using the exemplary custom-designed rigid electrodes from a single subject for "Reward” (blue line) using both the “vertical-sagittal” configuration (gradient potential configuration).
  • the exemplary custom-designed sensors can also adequately detect all tested ERPs in the "vertical-sagittal" configuration (gradient potential configuration), e.g., Targets vs.
  • the disclosed three-electrode frontal vertical-sagittal configuration is capable of efficient ERP detection using various type rigid electrodes.
  • FIG. 10 shows a schematic of an exemplary EES frontal three-electrode design 1000.
  • the exemplary EES frontal three-electrode design 1000 can be used to configure the electrodes of the device 100, as shown in the diagram of FIG. 1A .
  • the EES frontal three-electrode design 1000 includes a recording electrode 1001 structured to include ultrathin electrode islands 1010 with protruding, serpentine-like wires 1011, which all rest on a biologically inert, flexible, stretchable, and/or conforming substrate (e.g., polymer).
  • a biologically inert, flexible, stretchable, and/or conforming substrate e.g., polymer
  • the EES frontal three-electrode design 1000 includes a ground electrode 1002 separated from the recording electrode 1001 on the substrate by a first distance (e.g., in this example, 12.0 mm) and structured to include the electrode islands 1010 and the protruding, serpentine-like wires 1011.
  • the EES frontal three-electrode design 1000 includes a reference electrode 1003 separated from the ground electrode 1002 on the substrate by a second distance (e.g., in this example, 12.0 mm) and structured to include the electrode islands 1010 and the protruding, serpentine-like wires 1011.
  • the arrangement of the recording electrode 1001, ground electrode 1002, and the reference electrode 1003 are aligned in the sagittal direction.
  • the electrode island structures 1010 are configured to have two perpendicular ends, where one end is aligned in parallel with the protruding, serpentine-like wires 1011 and having a 3.0 mm size, while the other end is aligned perpendicular with the protruding, serpentine-like wires 1011 and having a 6.3 mm size.
  • Other examples of the exemplary EES frontal three-electrode design 1000 can include different sizes and spacings of the electrode structures.
  • the two exemplary frontal configurations horizontal anatomical alignment of the electrodes along the transverse direction and the vertical anatomical alignment of the electrodes along the sagittal direction, were implemented using the flexible EES sensors.
  • the three sensors were placed from the top of the forehead towards the nose, as follows: “Recording F1" electrode, "Ground” electrode, "Reference” electrode, as shown in FIG. 11A .
  • the three sensors were placed along the forehead from left to right, as follows: “Reference” electrode, "Ground” electrode, "Recording F1” electrode, as shown in FIG. 11B .
  • Exemplary implementations of the disclosed frontal electrode physiological sensor configurations were performed using an epidermal electronics system.
  • the subject's forehead was first cleaned using an alcohol swab and sterile gauze.
  • exemplary three-electrode EES flexible sensor devices were placed on the subject's forehead.
  • Each of three sheets of ACF was electrically coupled to a DIN cable on one end and electrically bonded to the EES device's interface pads on the other, aimed toward the subject's right hand side.
  • the subject was instructed to tilt his/her head back as the EES device was wet with tap water using a curved, plastic syringe.
  • the subject used a paper towel to cover their eyes from the water.
  • the EES device was gently rubbed until it adhered and was flush with the subject's forehead.
  • a no-sting liquid bandage was used to more firmly bond the EES device to the forehead.
  • the EES device's DIN cables were taped to the subject's head using masking tape. For example, this prevented the cables from falling into the subject's field of view and also prevented the cables from pulling on the EES device itself. Also for example, the DIN cables were clipped to the subject's shirt collar to prevent pulling. The DIN cables were subsequently plugged into a traditional EEG amplification system.
  • FIG. 12 shows data plots of an exemplary EEG online recording acquired using the exemplary EES flexible electrodes before stimuli presentation for both gradient potential and isopotential configurations.
  • the data plot 1210 shows the exemplary EEG data for the isopotential configuration of the exemplary three-electrode frontal flexible EES sensors.
  • the data plot 1220 shows the exemplary EEG response data for the gradient potential configuration of the exemplary three-electrode frontal flexible EES sensors. Eye blinks were used to better illustrate the signal-to-noise (SNR) ratio of the response in this example.
  • SNR signal-to-noise
  • FIG. 13 shows data plots of an exemplary EEG online recording acquired using the exemplary EES flexible electrodes during an exemplary stimuli presentation for both gradient potential and isopotential configurations.
  • the data plot 1310 shows the exemplary EEG data for the isopotential configuration of the exemplary three-electrode EES flexible sensors.
  • the data plot 1320 shows the exemplary EEG response data for the gradient potential configuration of the exemplary three-electrode EES flexible sensors. Eye blinks were used to better illustrate the signal-to-noise (SNR) ratio of the response in this example.
  • SNR signal-to-noise
  • FIG. 14A shows an exemplary data plot of ERP waveforms acquired using the exemplary EES flexible electrodes from a single subject for "Targets" (red line) and “Distractors” (black line) using both the “vertical-sagittal” configuration (gradient potential configuration, shown by thicker lines) and the “horizontal-transverse” configuration (isopotential configuration, shown by thinner lines).
  • FIG. 14B shows an exemplary data plot of ERP waveforms acquired using the exemplary EES flexible electrodes from a single subject for "Reward” (blue line) using both the “vertical-sagittal” configuration (gradient potential configuration, shown by thicker lines) and the “horizontal-transverse” configuration (isopotential configuration, shown by thinner lines).
  • the disclosed three-electrode frontal configuration using the gradient potential configuration is capable of efficient ERP detection using EES flexible electrodes.
  • Mismatch negativity is an ERP modulation that can be correlated with a wide range of neurological and neuropsychiatric disorders. MMN is thought to reflect pre-attentive detection of a deviant stimulus and can be calculated as the difference wave between the responses to deviants (e.g., infrequent) and to standard (e.g., frequent) stimuli in an 'oddball' paradigm.
  • deviants e.g., infrequent
  • standard (e.g., frequent) stimuli in an 'oddball' paradigm For example, scientific studies on patients suffering from a variety of mental disorders, e.g., including schizophrenia, Alzheimer's disease, and autism spectrum disorder (ASD), have systematically reported that these patient show a decreased ability to detect novel stimuli than healthy subjects. Consistent with this behavior deficit, the amplitude of the MMN is reduced, and thus the MMN can be treated as a marker of either progressive pathology or vulnerability for these disorders.
  • ASSD autism spectrum disorder
  • FIG. 15 shows a diagram of an exemplary sequence of stimuli for the MMN oddball paradigm.
  • the 'S' represents a standard stimulus and 'D' represents a deviant stimulus.
  • deviants were used 20%, and standards were used 80%.
  • condition 1 standard-low and deviant high
  • condition 2 standard-high and deviant low.
  • condition 1 standard-low and deviant high
  • condition 2 standard-high and deviant low.
  • 1040 trials e.g., standards and deviants (ratio of deviants to standards was 1:4)
  • FIG. 16A shows a data plot of exemplary group average (e.g., from 5 subjects) of ERP waveforms of the elicited MMN (black line), deviants (red line) and standards (blue line
  • Implementations of the subject matter and the functional operations described in this patent document can be implemented in various systems, digital electronic circuitry, or in computer software, firmware, or hardware, including the structures disclosed in this specification and their structural equivalents, or in combinations of one or more of them. Implementations of the subject matter described in this specification can be implemented as one or more computer program products, i.e., one or more modules of computer program instructions encoded on a tangible and non-transitory computer readable medium for execution by, or to control the operation of, data processing apparatus.
  • the computer readable medium can be a machine-readable storage device, a machine-readable storage substrate, a memory device, a composition of matter effecting a machine-readable propagated signal, or a combination of one or more of them.
  • data processing apparatus encompasses all apparatus, devices, and machines for processing data, including by way of example a programmable processor, a computer, or multiple processors or computers.
  • the apparatus can include, in addition to hardware, code that creates an execution environment for the computer program in question, e.g., code that constitutes processor firmware, a protocol stack, a database management system, an operating system, or a combination of one or more of them.
  • a computer program (also known as a program, software, software application, script, or code) can be written in any form of programming language, including compiled or interpreted languages, and it can be deployed in any form, including as a stand-alone program or as a module, component, subroutine, or other unit suitable for use in a computing environment.
  • a computer program does not necessarily correspond to a file in a file system.
  • a program can be stored in a portion of a file that holds other programs or data (e.g., one or more scripts stored in a markup language document), in a single file dedicated to the program in question, or in multiple coordinated files (e.g., files that store one or more modules, sub programs, or portions of code).
  • a computer program can be deployed to be executed on one computer or on multiple computers that are located at one site or distributed across multiple sites and interconnected by a communication network.
  • the processes and logic flows described in this specification can be performed by one or more programmable processors executing one or more computer programs to perform functions by operating on input data and generating output.
  • the processes and logic flows can also be performed by, and apparatus can also be implemented as, special purpose logic circuitry, e.g., an FPGA (field programmable gate array) or an ASIC (application specific integrated circuit).
  • processors suitable for the execution of a computer program include, by way of example, both general and special purpose microprocessors, and any one or more processors of any kind of digital computer.
  • a processor will receive instructions and data from a read only memory or a random access memory or both.
  • the essential elements of a computer are a processor for performing instructions and one or more memory devices for storing instructions and data.
  • a computer will also include, or be operatively coupled to receive data from or transfer data to, or both, one or more mass storage devices for storing data, e.g., magnetic, magneto optical disks, or optical disks.
  • mass storage devices for storing data, e.g., magnetic, magneto optical disks, or optical disks.
  • a computer need not have such devices.
  • Computer readable media suitable for storing computer program instructions and data include all forms of nonvolatile memory, media and memory devices, including by way of example semiconductor memory devices, e.g., EPROM, EEPROM, and flash memory devices.
  • semiconductor memory devices e.g., EPROM, EEPROM, and flash memory devices.
  • the processor and the memory can be supplemented by, or incorporated in, special purpose logic circuitry.

Claims (15)

  1. Dispositif de capteur physiologique (100) pour détecter des signaux physiologiques, comprenant :
    un substrat (101) formé d'un matériau électriquement isolant et structuré pour permettre un contact physique du dispositif avec la région frontale de la tête d'un utilisateur ;
    une première électrode (102) configurée à un premier emplacement sur le substrat (101) pour acquérir un signal électrophysiologique de l'utilisateur qui inclut un signal pertinent ;
    une deuxième électrode (103) configurée à un deuxième emplacement sur le substrat (101) pour acquérir un deuxième signal électrophysiologique de l'utilisateur comme un signal de référence au signal électrophysiologique de sorte que le signal de référence inclut une différence de potentiel pour faciliter la différenciation du signal pertinent ; et
    une troisième électrode (104) configurée sur le substrat (101) pour acquérir un troisième signal électrophysiologique de l'utilisateur comme un signal de masse électrique,
    dans lequel la troisième électrode (104) est configurée à un troisième emplacement au moins partiellement entre le premier et le deuxième emplacements sur le substrat (101), et le premier emplacement est configuré de de manière postérieure aux deuxième et troisième emplacements, et la première électrode (102), la deuxième électrode (103) et la troisième électrode (104) sont alignées le long d'une ligne droite le long d'une direction verticale au milieu de la région frontale lorsque le dispositif de capteur physiologique (100) est correctement placé sur le front de l'utilisateur, et
    dans lequel le dispositif peut être opéré lors de son couplage électrique à un circuit électrique (110) pour détecter des signaux physiologiques de l'utilisateur.
  2. Dispositif selon la revendication 1, dans lequel les première, deuxième et troisième électrodes (102, 103, 104) sont agencées linéairement sur le substrat (101).
  3. Dispositif selon la revendication 1, dans lequel les signaux physiologiques sont des signaux d'électroencéphalographie, EEG, captés à partir du cerveau de l'utilisateur et les signaux d'EEG détectés sont associés à un potentiel lié à l'événement, ERP.
  4. Dispositif selon la revendication 1, dans lequel les signaux physiologiques sont des signaux d'électromyographie, EMG, captés à partir de muscles de la tête de l'utilisateur associés au clignement de l'œil ou aux expressions faciales de l'utilisateur.
  5. Dispositif selon la revendication 1, dans lequel le substrat (101) est formé d'un matériau flexible mécaniquement structuré pour adhérer à la peau ou un article portable de l'utilisateur.
  6. Dispositif selon la revendication 5, comprenant en outre :
    des composants d'interface électrique (112a, 112b, 112c) formés séparément sur le substrat (101) et couplés électriquement aux première, deuxième et troisième électrodes (102, 103, 104), respectivement, par le biais de conduits électriquement conducteurs (111a, 111b, 111c),
    dans lequel le circuit électrique (110) est un circuit électrique externe couplé électriquement aux composants d'interface électrique par le biais de fils.
  7. Dispositif selon la revendication 5, dans lequel le circuit électrique (110) inclut :
    un circuit de traitement de signaux formé sur le substrat (101) en communication électrique avec les première, deuxième et troisième électrodes (102, 103, 104) par le biais de conduits électriquement conducteurs, le circuit de traitement de signaux étant destiné à amplifier les signaux physiologiques acquis, et
    un module émetteur sur le substrat (101) en communication électrique avec le circuit de traitement de signaux pour transmettre les signaux physiologiques amplifiés à au moins un d'un module de traitement de données ou d'un système informatique à distance.
  8. Dispositif selon la revendication 7, dans lequel le dispositif de capteur physiologique (100) est configuré comme un timbre portable porté sur le cuir chevelu de l'utilisateur.
  9. Dispositif selon la revendication 7, dans lequel le dispositif de capteur physiologique (100) est configuré dans une région de l'article portable capable de contact physique avec le cuir chevelu de l'utilisateur.
  10. Dispositif selon la revendication 1, comprenant en outre :
    une quatrième électrode configurée à un quatrième emplacement sur le substrat (101) pour acquérir un deuxième signal électrophysiologique de l'utilisateur ; et
    une cinquième électrode configurée à un cinquième emplacement sur le substrat (101) pour acquérir un troisième signal électrophysiologique de l'utilisateur,
    dans lequel le quatrième emplacement est configuré à gauche du premier emplacement et le cinquième emplacement est configuré à droite du premier emplacement.
  11. Dispositif selon la revendication 1 mis en œuvre dans un système pour fournir une évaluation cognitive ou sensorielle, dans lequel le système comprend :
    un système de traitement de données en communication avec le dispositif de capteur physiologique (100) et structuré pour inclure un ou plusieurs modules de mémoire et un ou plusieurs processeurs configurés pour traiter les signaux physiologiques détectés comme données physiologiques pour générer un ensemble d'informations incluant une ou plusieurs valeurs quantitatives associées à une catégorie de profil cognitif-sensoriel indicatrice d'un ou plusieurs aspects de fonctions cognitives ou sensorielles.
  12. Dispositif selon la revendication 11, dans lequel le ou les processeurs du module de traitement de données sont configurés pour traiter les signaux physiologiques détectés par le dispositif de capteur physiologique (100) pour générer l'ensemble d'informations en :
    sélectionnant des intervalles de temps pertinents au sein des données physiologiques en fonction des stimuli présentés et de la catégorie de profil cognitif-sensoriel,
    regroupant, en un ou plusieurs ensembles de données regroupées, les données physiologiques correspondant aux intervalles de temps pertinents sélectionnés, et
    fournissant une mesure statistique d'une relation en travers ou au sein des ensembles de données regroupées pour générer la ou les valeurs quantitatives.
  13. Dispositif selon la revendication 11, dans lequel le système comprend en outre :
    un dispositif de fourniture de stimuli (135) pour produire une séquence de stimuli basée sur la catégorie de profil cognitif-sensoriel qui est présentée à l'utilisateur portant le dispositif de capteur physiologique (100), dans lequel les stimuli incluent au moins un d'un support de stimulation visuelle, auditive, olfactive, tactile ou gustative,
    dans lequel le dispositif de capteur physiologique (100) est interfacé à l'utilisateur pour détecter les signaux physiologiques présentés par l'utilisateur avant, au cours de et après une présentation de la séquence de stimuli.
  14. Procédé pour fournir une évaluation cognitive ou sensorielle d'un sujet, comprenant :
    acquérir des signaux électrophysiologiques du sujet à partir de la région frontale de la tête du sujet pour produire des données physiologiques en utilisant un dispositif de capteur (100) incluant :
    un substrat (101) formé d'un matériau électriquement isolant et structuré pour permettre un contact physique du dispositif de capteur (100) avec la région frontale de la tête du sujet, et
    trois électrodes incluant une électrode d'enregistrement (102), une électrode de référence (103) et une électrode de masse (104) pour acquérir les signaux électrophysiologiques du sujet à partir de trois positions respectives agencées sur le substrat (101), les positions incluant l'électrode de masse (104) configurée entre l'électrode d'enregistrement (102) et l'électrode de référence (103) de sorte que les trois électrodes sont alignées le long d'une ligne droite le long d'une direction verticale au milieu de la région frontale lorsque le dispositif de capteur physiologique (100) est placé sur le front du sujet, dans lequel l'électrode d'enregistrement (102) est configurée de manière postérieure aux électrodes de masse et de référence (104, 103) pour acquérir un signal électrophysiologique du sujet qui inclut un signal pertinent de sorte qu'un signal de référence acquis par l'électrode de référence (103) inclut une différence de potentiel pour faciliter la différenciation du signal pertinent ; et
    traiter les données physiologiques pour générer un ensemble d'informations incluant une ou plusieurs valeurs quantitatives associées à une catégorie de profil cognitif-sensoriel indicatrice d'un ou plusieurs aspects de fonctions cognitives ou sensorielles.
  15. Procédé selon la revendication 14, comprenant en outre :
    présenter une séquence de stimuli au sujet, la séquence de stimuli étant basée sur la catégorie de profil cognitif-sensoriel,
    dans lequel l'acquisition des signaux électrophysiologiques est mise en œuvre avant, au cours de et après la présentation de la séquence de stimuli.
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US20150313498A1 (en) 2015-11-05
EP2906115A4 (fr) 2016-05-25
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CA2887535A1 (fr) 2014-04-17
JP6454944B2 (ja) 2019-01-23
BR112015008043A2 (pt) 2017-07-04
WO2014059431A3 (fr) 2014-06-19
CN104902814B (zh) 2018-03-02
CN104902814A (zh) 2015-09-09
EP2906115A2 (fr) 2015-08-19
CA2887535C (fr) 2021-03-09
US10182736B2 (en) 2019-01-22
WO2014059431A2 (fr) 2014-04-17
KR20150098607A (ko) 2015-08-28
JP2015534842A (ja) 2015-12-07

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